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Reproductive Health
Pre-Implantation Genetic Testing/Screening (PGT/PGS)
Reproductive Health Tests
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Screening Embryos for Healthier Pregnancies and Healthier Generations
PGT/PGS is a genetic testing method performed during IVF to evaluate embryos for chromosomal abnormalities or inherited conditions. This helps increase pregnancy success rates, reduce the risk of genetic disorders, and empower families with informed decisions before implantation.
Conditions Detected by PGT/PGS
01
Chromosomal Aneuploidies
02
Single-Gene Disorders
03
Structural Rearrangements
04
Sex Chromosome Abnormalities
Why PGT/PGS is a Game Changer
Higher IVF Success
Improves embryo selection for a greater chance of healthy pregnancy outcomes.
Genetic Clarity
Avoids passing on known genetic conditions to the next generation.
Informed Choices
Empowers couples with data to make confident family planning decisions.
Reduced Miscarriages
Selects chromosomally normal embryos to lower risk of early pregnancy loss.
How Does PGT/PGS Work?
A quick and precise genetic screening during IVF embryo development.
Embryo Biopsy
A few cells are carefully removed from the embryo on day 5 or 6.
Genetic Analysis
Cells are analyzed in our advanced lab for chromosomal or genetic conditions.
Embryo Selection
Only healthy embryos are chosen for implantation, enhancing IVF success.
Why Choose FSG for PGT/PGS
01
Advanced Screening
We use comprehensive PGT-A and PGT-M panels for detailed embryo analysis.
02
IVF Collaboration
Seamless integration with IVF clinics to ensure safe and effective testing.
03
Fast Reporting
Receive results in just a few days to support timely embryo transfer.
04
Trusted Genetics Lab
FSG is a UAE-certified genomics leader with a reputation for accuracy and care.
FAQ’s
Frequently Asked Questions!
We’re here to help. Explore answers or reach out to our team directly.
PGT/PGS is a procedure used during IVF to screen embryos for genetic abnormalities before implantation. It helps identify healthy embryos, increasing the chances of a successful pregnancy.
It is often recommended for couples with a history of genetic disorders, recurrent miscarriages, advanced maternal age, or previous failed IVF attempts.
Yes, the biopsy is done at a stage where it does not harm the embryo's development. It is performed by highly trained specialists using advanced techniques.
PGT can detect chromosomal abnormalities (like Down syndrome) and specific inherited genetic disorders, depending on the test type (PGT-A, PGT-M, or PGT-SR).
While it significantly reduces the risk of genetic issues, it cannot guarantee a completely healthy baby. It improves the likelihood of a successful and healthy pregnancy.
Non-Invasive Prenatal Testing/Screening
Pre-Implantation Genetic Testing/Screening (PGT/PGS)
Male/Female Fertility
Rapid Prenatal & Pregnancy Loss
Maternal Cell Contamination (MCC)
Product of Conception (POC)
My HLA (Human Leucocyte Antigen)
Whole Genome Sequencing (WGS)
Whole Exome Sequencing (WES)
Low Pass Sequencing (1-3x Coverage)
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Breast Cancer Screening (BRCA)
Cervical Cancer Screening
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